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Integration of FDA and NIOSH Processes Used to Evaluate Respiratory Protective Devices for Health Care Workers Proceedings of a Workshop (2017) / Chapter Skim
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References
Pages 49-50

The Chapter Skim interface presents what we've algorithmically identified as the most significant single chunk of text within every page in the chapter.
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From page 49...
... 2016. Use of International Standard ISO 10993-1, "Biological evaluation of medical devices -- Part 1: Evaluation and testing within a risk management process." Guidance for industry and Food and Drug Administration staff.
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From page 50...
... 2015. Resistance to synthetic blood penetration of National Institute for Occupational Safety and Health-approved N95 filtering facepiece respirators and surgical N95 respirators.
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Key Terms

  • environmental hygiene
  • facepiece respirators
  • occupational safety
  • accessed september
  • respiratory protection

  • respirator filtration
  • administration staff
  • filtering facepieces
  • filtration test
  • respirator certification

  • hospital respiratory
  • blood penetration
  • association journal
  • influenza virus
  • synthetic blood

  • biological agents
  • american industrial
  • industrial hygiene
  • facepiece particulate
  • certification tell

  • containing viable
  • seal interface
  • hygiene association
  • reduce inhalation
  • implementing hospital

  • airborne biological
  • accessed december
  • joint commission
  • national institute
  • drug administration


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